Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
-/CCGACCTT
Location

Chromosome 1: between 219926483 and 219926484 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs397955342

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts.

Variant displays